Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 transcript reference sequence.

15 entries on 1 page. Showing entries 1 - 15.
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+/? 10 c.1724G>A r.(?) p.(Cys575Tyr) - Maternal (confirmed) - pathogenic g.216465633C>T g.216292291C>T - - USH2A_000344 - PubMed: de Castro-Miró 2016 - - Germline yes - - - - DNA SEQ-NG-I Blood - RP39 51ORG PubMed: de Castro-Miró 2016 - M ? Spain white - - - - 2 Marta de Castro-Miró
+/? 10 c.1724G>A r.(?) p.(Cys575Tyr) Laminin EGF-like 2 (575-640) Paternal (confirmed) ACMG likely pathogenic g.216465633C>T g.216292291C>T - - USH2A_000344 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 10 c.1724G>A r.(?) p.(Cys575Tyr) Laminin EGF-like 2 (575-640) Paternal (confirmed) ACMG likely pathogenic g.216465633C>T g.216292291C>T - - USH2A_000344 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 10 c.1724G>A r.(?) p.(Cys575Tyr) Laminin EGF-like 2 (575-640) Parent #2 ACMG likely pathogenic g.216465633C>T g.216292291C>T - - USH2A_000344 Heterozygous; Presumably pathogenic PubMed: Bonnet 2011, USMA missense analysis, missense variant in MSV3d - - Germline - 0/306 controls none - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/. - c.1724G>A r.(?) p.(Cys575Tyr) - Parent #2 - pathogenic g.216465633C>T g.216292291C>T - - USH2A_000344 - - - - Germline - - - - - DNA SEQ-NG-I Peripheral blood - retinal disease - - - M - - - - - - - 4 Marta de Castro-Miró
+?/. - c.1724G>A r.(?) p.(Cys575Tyr) - Both (homozygous) - likely pathogenic g.216465633C>T g.216292291C>T - - USH2A_000344 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 102 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.1724G>A r.(?) p.(Cys575Tyr) - Unknown ACMG VUS g.216465633C>T - - - USH2A_000344 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GS_0155 - - M - Korea, South (Republic) - - - - - 1 Jinu Han
?/. - c.1724G>A r.(?) p.(Cys575Tyr) - Unknown - VUS g.216465633C>T g.216292291C>T c.1724G>A, p.Cys575Tyr - USH2A_000344 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2865_004450 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.1724G>A r.(?) p.(Cys575Tyr) - Parent #1 - likely pathogenic g.216465633C>T g.216292291C>T USH2A c.1724G>A, p.C575Y - USH2A_000344 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 144 PubMed: Jauregui 2020 - M - (United States) Hispanic - - - - 1 LOVD
+?/. - c.1724G>A r.(?) p.(Cys575Tyr) - Maternal (confirmed) ACMG likely pathogenic g.216465633C>T - - - USH2A_000344 - PubMed: Mansard et al, 2021 - rs483353054 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.1724G>A r.(?) p.(Cys575Tyr) - Unknown ACMG likely pathogenic g.216465633C>T - - - USH2A_000344 - PubMed: Mansard et al, 2021 - rs483353054 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. 10 c.1724G>A r.(?) p.(Cys575Tyr) - Unknown - likely pathogenic g.216465633C>T - p.C575Y - USH2A_000344 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 10 c.1724G>A r.(?) p.(Cys575Tyr) - Unknown - likely pathogenic g.216465633C>T - p.C575Y - USH2A_000344 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. - c.1724G>A r.(?) p.(Cys575Tyr) - Parent #2 - pathogenic g.216465633C>T g.216292291C>T USH2A c.1724G>A, p.Cys575Tyr - USH2A_000344 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD17111461 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. - c.1724G>A r.(?) p.(Cys575Tyr) - Unknown ACMG pathogenic g.216465633C>T g.216292291C>T - - USH2A_000344 ACMG GN005 criteria: PM2_P PM3_VS PP3_P PubMed: Gao, F. J. et al., 2021; PubMed: Cabanillas, R. et al., 2018; PubMed: Wafa, T. T. et al., 2021; PubMed: Mansard, L. et al., 2021; PubMed: Jauregui, R. et al., 2020 - rs483353054 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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